MeSH keywords -> Related genes, diseases (OMIM)
Query MeSH keywords list
01
Hydroxybutyrates
[NCBI]
Gene
Gene
Link
Information
Gain
01
MS
[NCBI]
5.5892e-05
ALDH5A1
[NCBI]
5.34133e-05
OXCT2
[NCBI]
2.1099e-05
LPL
[NCBI]
8.01517e-06
ACAT1
[NCBI]
5.91714e-06
ADHFE1
[NCBI]
4.92119e-06
PTGS2
[NCBI]
3.10347e-06
GIP
[NCBI]
2.39389e-06
SLC2A1
[NCBI]
2.1931e-06
HIBADH
[NCBI]
2.16342e-06
BDH1
[NCBI]
2.07331e-06
D2HGDH
[NCBI]
2.04895e-06
DHODH
[NCBI]
1.96907e-06
SLC16A3
[NCBI]
1.95234e-06
SLC16A7
[NCBI]
1.84658e-06
PDK2
[NCBI]
1.83588e-06
SLC5A8
[NCBI]
1.78799e-06
PDK4
[NCBI]
1.76289e-06
SLC16A4
[NCBI]
1.68102e-06
EGF
[NCBI]
1.54781e-06
PC
[NCBI]
1.39337e-06
CAD
[NCBI]
1.32035e-06
C3
[NCBI]
1.31286e-06
ACHE
[NCBI]
1.29456e-06
SCP2
[NCBI]
1.17432e-06
HCFC1
[NCBI]
1.12193e-06
CS
[NCBI]
1.11413e-06
POU2F1
[NCBI]
1.10117e-06
MMP13
[NCBI]
1.05045e-06
SLC2A4
[NCBI]
9.61354e-07
TNF
[NCBI]
7.58214e-07
IL6
[NCBI]
7.14744e-07
IL1RN
[NCBI]
6.52955e-07
MPO
[NCBI]
5.62297e-07
AVP
[NCBI]
5.3415e-07
VIP
[NCBI]
5.34078e-07
CCK
[NCBI]
5.12721e-07
PCNA
[NCBI]
5.06416e-07
TH
[NCBI]
4.94968e-07
PRL
[NCBI]
3.77121e-07
OMIM
OMIM
Link
Information
gain
01
3-@hydroxyisobutyric aciduria
[NCBI]
0.00541205
methionine malabsorption syndrome
[NCBI]
0.00179377
carnitine deficiency, myopathic
[NCBI]
0.00141752
succinic semialdehyde dehydrogenase deficiency
[NCBI]
0.00141432
alpha-methylacetoacetic aciduria
[NCBI]
0.000484201
succinyl-coa:3-oxoacid coa transferase deficiency
[NCBI]
0.000220078
lactic acidosis, chronic adult form
[NCBI]
0.00017125
LS
[NCBI]
0.000128232
ALDH5A1
[NCBI]
0.000114317
hydroxyacyl-coa dehydrogenase ii deficiency
[NCBI]
0.000105902
donohue syndrome
[NCBI]
8.47774e-05
acyl-coa dehydrogenase, short-chain, deficiency of
[NCBI]
8.2194e-05
LPL
[NCBI]
8.1306e-05
pyruvate carboxylase deficiency
[NCBI]
8.10063e-05
ADHFE1
[NCBI]
8.01139e-05
acyl-coa dehydrogenase, medium-chain, deficiency of
[NCBI]
7.02231e-05
mitochondrial complex iv deficiency
[NCBI]
6.75477e-05
ACAT1
[NCBI]
6.34278e-05
pyruvate decarboxylase deficiency
[NCBI]
6.30142e-05
RA
[NCBI]
4.37472e-05
OXCT1
[NCBI]
3.29367e-05
PCCA
[NCBI]
2.61629e-05
3-@hydroxy-3-methylglutaryl-coa lyase deficiency
[NCBI]
2.49441e-05
GIP
[NCBI]
2.4593e-05
SLC16A1
[NCBI]
2.16448e-05
DAO
[NCBI]
2.02188e-05
PC
[NCBI]
1.63994e-05
IL6
[NCBI]
1.4225e-05
GPI
[NCBI]
1.08418e-05
hla-d histocompatibility type
[NCBI]
8.58727e-06
ACHE
[NCBI]
5.01414e-06
EGF
[NCBI]
2.62163e-06
MPO
[NCBI]
1.45045e-06
VIP
[NCBI]
1.04962e-06
PCNA
[NCBI]
8.34258e-07
CCK
[NCBI]
8.31621e-07
TH
[NCBI]
6.64353e-07
AVP
[NCBI]
5.7984e-07
TNF
[NCBI]
2.4702e-07
PRL
[NCBI]
1.01243e-08
Database Center for Life Science